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Pulpotomy vs Root Canal Treatment for Teeth With Symptomatic Irreversible Pulpitis

B

British University In Egypt

Status

Enrolling

Conditions

Pulpitis - Irreversible

Treatments

Procedure: vital pulp therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05726357
FD BUE REC 22-034

Details and patient eligibility

About

high-quality evidence is needed to add to current knowledge and also assess the long-term outcomes for full/complete pulpotomy after carious pulpal exposure in patients with signs and symptoms indicative of irreversible pulpitis

Enrollment

380 estimated patients

Sex

All

Ages

12+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • a mature permanent tooth
  • symptoms indicative of IRP
  • responsive to cold and EPT sensibility testing
  • restorable and can be adequately isolated during treatment
  • One tooth (molar or premolar) per patient.

Exclusion criteria

  • active periodontal disease
  • complex medical histories
  • unable to consent
  • pregnant or breast-feeding
  • excessive bleeding that cannot be controlled

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

380 participants in 2 patient groups

standard root canal treatment
Active Comparator group
Description:
standard root canal treatment
Treatment:
Procedure: vital pulp therapy
Pulpotomy
Active Comparator group
Description:
vital pulp therapy
Treatment:
Procedure: vital pulp therapy

Trial contacts and locations

1

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Central trial contact

Shehabeldin Saber, phD; Dalia Ghalwash, phD

Data sourced from clinicaltrials.gov

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